Quality Assurance Centre
Our Quality Assurance Centre is both a physical and digital infrastructure dedicated to ensuring that every product we manufacture meets rigorous quality standards. Key components include:
Analytical Laboratories – Equipped with advanced instrumentation (HPLC, GC‑MS, FTIR, UV spectrophotometry) for testing raw materials and finished products. These labs support identity verification, potency assays, contamination checks and shelf‑life studies.
Microbiology Facilities – Separate clean rooms and microbiology labs conduct tests for microbial contamination (e.g., total plate count, yeast and mold, pathogens). We follow pharmacopeial standards and maintain validated methods.
Stability Chambers – Controlled environments simulate various storage conditions to determine product stability and recommended shelf life. Stability studies adhere to International Council for Harmonisation (ICH) guidelines for nutraceuticals and cosmetics.
Documentation & Digital Systems – We employ electronic quality‑management systems (eQMS) integrated with our Enterprise Resource Planning (ERP) platform. This integration allows batch tracking, traceability, deviations management, CAPA (corrective and preventive actions) and real‑time quality monitoring. Blockchain or serialized coding may be used for enhanced traceability, if requested by clients.
Qualified Personnel – Our quality team includes pharmacists, chemists, microbiologists and regulatory specialists with experience in global compliance. They conduct regular internal audits, manage regulatory inspections and oversee continuous improvement initiatives.
Client Audits – We welcome audits by existing or prospective clients under mutual confidentiality agreements. Our Quality Assurance Centre provides transparent documentation and facilitates regulatory and supplier qualification audits.
